Gaois

Cóip statach de shonraí a easpórtáiltear ó IATE ó am go chéile atá sa chnuasach seo. Níor cheart glacadh leis gurb ionann i gcónaí an t-eolas a thugtar faoi iontráil anseo agus a bhfuil sa leagan reatha den iontráil ar IATE. Is féidir an leagan reatha sin a cheadú ach cliceáil ar an nasc atá ar thaobh na láimhe deise ag barr gach iontrála. Breis eolais »

3 thoradh

  1. INDUSTRY|industrial structures and policy|industrial production|industrial product · TRADE|consumption|consumer|consumer protection · PRODUCTION, TECHNOLOGY AND RESEARCH|technology and technical regulations|technical regulations · EUROPEAN UNION|European Union law|EU law
    deimhniú de chuid an Aontais Eorpaigh ar dhearadhscrúdú Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    EG-Entwurfsprüfbescheinigung | EU-Entwurfsprüfbescheinigung
    de
    EC design examination certificate | EU design examination certificate | EU design-examination certificate
    en
    Sainmhíniú "certificate issued by a notified body after having assessed the quality system and the product design (module H1)" Tagairt "COM-Terminology Coordination, based on: Commission notice The ‘Blue Guide’ on the implementation of EU product rules 2022 2022/C 247/01"
    Nóta "Both ""EC design examination certificate"" and ""EU design examination certificate"" are used.The EU-design examination certificate must not be confused with the EU-type examination certificate of module B that attests the conformity of a specimen ‘representative of the production envisaged’, so that the conformity of the products may be checked against this specimen."
  2. EDUCATION AND COMMUNICATIONS|information technology and data processing|computer system|information security
    clár oibre rollach de chuid an Aontais Tagairt "Rialachán (AE) 2019/881 ó Pharlaimint na hEorpa agus ón gComhairle maidir le ENISA (Gníomhaireacht an Aontais Eorpaigh um Chibearshlándáil) agus maidir le deimhniú i ndáil le cibearshlándáil theicneolaíocht na faisnéise agus na cumarsáide"
    ga
    Comhthéacs Ba cheart don Choimisiún clár oibre rollach de chuid an Aontais do scéimeanna Eorpacha um dheimhniú cibearshlándála a ullmhú le tacaíocht an Ghrúpa Eorpaigh um Dheimhniú Cibearshlándála (“an ECCG”) agus Ghrúpa na nGeallsealbhóirí um Dheimhniú Cibearshlándála, tar éis comhairliúchán oscailte ar fud an Aontais agus ba cheart don Choimisiún é a fhoilsiú i bhfoirm ionstraime atá neamhcheangailteach. Tagairt "Rialachán (AE) 2019/881 ó Pharlaimint na hEorpa agus ón gComhairle maidir le ENISA (Gníomhaireacht an Aontais Eorpaigh um Chibearshlándáil) agus maidir le deimhniú i ndáil le cibearshlándáil theicneolaíocht na faisnéise agus na cumarsáide"
    clár oibre rollach de chuid an Aontais le haghaidh deimhniú Eorpach cibearshlándála Tagairt "Comhairle-GA, bunaithe ar 'clár oibre rollach de chuid an Aontais do scéimeanna Eorpacha um dheimhniú cibearshlándála' in Rialachán (AE) 2019/881"
    ga
    fortlaufendes Arbeitsprogramm der Union für die europäische Cybersicherheitszertifizierung | fortlaufendes Arbeitsprogramm der Union
    de
    Sainmhíniú "von der Kommission zu veröffentlichendes Programm, in dem die strategischen Prioritäten für künftige europäische Schemata für die Cybersicherheitszertifizierung IATE:3574165 festgelegt werden" Tagairt "Council-DE nach Verordnung (EU) 2019/881 des Europäischen Parlaments und des Rates vom 17. April 2019 über die ENISA (Agentur der Europäischen Union für Cybersicherheit) und über die Zertifizierung der Cybersicherheit von Informations- und Kommunikationstechnik und zur Aufhebung der Verordnung (EU) Nr. 526/2013, Art.47 Abs.1"
    Nóta Umfasst insbesondere eine Liste der IKT-Produkte, -Dienste und -Prozesse oder Kategorien davon, die von der Aufnahme in ein europäisches Schema für die Cybersicherheitszertifizierung profitieren können.
    Union rolling work programme | Union rolling work programme for European cybersecurity certification
    en
    Sainmhíniú strategic non-binding document that allows industry, national authorities and standardisation bodies, in particular, to prepare in advance for future European cybersecurity certification schemes Tagairt "Council-DA, based on Regulation (EU) 2019/881 on ENISA (the European Union Agency for Cybersecurity) and on information and communications technology cybersecurity certification (Cybersecurity Act)"
    programme de travail glissant de l'Union | programme de travail glissant de l'Union pour la certification européenne de cybersécurité
    fr
    Sainmhíniú "document stratégique non contraignant permettant aux entreprises du secteur, aux autorités nationales et aux organismes de normalisation, en particulier, de se préparer à l'avance dans la perspective des futurs schémas européens de certification de cybersécurité et devant comporter un aperçu pluriannuel des demandes de schémas candidats que la Commission compte adresser à l'ENISA pour préparation, sur la base de motifs spécifiques" Tagairt "Conseil-FR, d'après le règlement (UE) 2019/881 relatif à l'ENISA (Agence de l'Union européenne pour la cybersécurité) et à la certification de cybersécurité des technologies de l'information et des communications (règlement sur la cybersécurité)"
  3. SOCIAL QUESTIONS|health|pharmaceutical industry
    deimhniú oiriúnachta leis na monagraif de chuid Pharmacopoeia Eorpach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Laistigh den nós imeachta le haghaidh ‘Deimhniú Oiriúnachta leis na monagraif de chuid Pharmacopoeia Eorpach’, fíoraíonn an Stiúrthóireacht Eorpach um Cháilíocht Leigheasra agus Cúraim Sláinte trí bhíthin cigireachtaí cibé acu a dheimhnítear nó nach ndeimhnítear leis na sonraí arna gcur isteach ag an iarratasóir arna bhunú ag Comhairle na hEorpa oiriúnacht monagraf chun an íonacht cheimiceach ...' Tagairt "Togra le haghaidh Treoir maidir le Cód an Aontais a bhaineann le táirgí íocshláinte lena n‑úsáid ag an duine, agus lena n‑aisghairtear Treoir 2001/83/CE agus Treoir 2009/35/CE, CELEX:52023PC0192/GA"
    Certification of Suitability to the monographs of the European Pharmacopoeia
    en
    Sainmhíniú procedure established in 1994 for the control of the chemical purity of pharmaceutical substances, of products posing a risk of transmitting transmissible spongiform encephalopathy as well as of herbal drugs and herbal drug preparations Tagairt "COM-Terminology Coordination, based on: Council of Europe. European Directorate for the Quality of Medicines & HealthCare. Medicines Certification of Suitability (CEP). About the Procedure. 'Certification - Background & Legal Framework' (19.6.2023)"